A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450267



Internal ID21107820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132752541..132948682hg38UCSC Ensembl
chr10:134566045..134762186hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38196142
hg19196142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv920n223
Supporting Variantsnssv18182854
Samples
Known GenesINPP5A, NKX6-2, TTC40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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